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The Inhibitory Effect of Non-Substrate and Substrate DNA on the Ligation and Self-Adenylylation Reactions Catalyzed by T4 DNA Ligase

机译:非底物和底物DNA对T4 DNA连接酶催化的连接和自腺苷酸化反应的抑制作用

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摘要

DNA ligases are essential both to in vivo replication, repair and recombination processes, and in vitro molecular biology protocols. Prior characterization of DNA ligases through gel shift assays has shown the presence of a nick site to be essential for tight binding between the enzyme and its dsDNA substrate, with no interaction evident on dsDNA lacking a nick. In the current study, we observed a significant substrate inhibition effect, as well as the inhibition of both the self-adenylylation and nick-sealing steps of T4 DNA ligase by non-nicked, non-substrate dsDNA. Inhibition by non-substrate DNA was dependent only on the total DNA concentration rather than the structure; with 1 μg/mL of 40-mers, 75-mers, or circular plasmid DNA all inhibiting ligation equally. A >15-fold reduction in T4 DNA ligase self-adenylylation rate when in the presence of high non-nicked dsDNA concentrations was observed. Finally, EMSAs were utilized to demonstrate that non-substrate dsDNA can compete with nicked dsDNA substrates for enzyme binding. Based upon these data, we hypothesize the inhibition of T4 DNA ligase by non-nicked dsDNA is direct evidence for a two-step nick-binding mechanism, with an initial, nick-independent, transient dsDNA-binding event preceding a transition to a stable binding complex in the presence of a nick site.
机译:DNA连接酶对于体内复制,修复和重组过程以及体外分子生物学方案都是必不可少的。通过凝胶位移测定法对DNA连接酶的先前表征已表明,缺口位点的存在对于酶与其dsDNA底物之间的紧密结合至关重要,而缺少缺口的dsDNA上没有明显的相互作用。在当前的研究中,我们观察到了显着的底物抑制作用,以及无缺口,无底物的dsDNA对T4 DNA连接酶的自腺苷酸化和切口密封步骤的抑制作用。非底物DNA的抑制作用仅取决于总DNA浓度,而不取决于结构。用1μg/ mL的40聚体,75聚体或环状质粒DNA均能同样抑制连接。当存在高非缺口dsDNA浓度时,观察到T4 DNA连接酶自腺苷酸化速率降低了> 15倍。最后,利用EMSA证明非底物dsDNA可以与带切口的dsDNA底物竞争酶结合。根据这些数据,我们假设非缺口dsDNA对T4 DNA连接酶的抑制作用是两步缺口结合机制的直接证据,其初始,缺口独立,短暂的dsDNA结合事件在过渡到稳定之前在缺刻部位存在的结合复合物。

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